Wu Li

MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype

Yong Feng, L. Mei, Hongsheng Chen, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

D. Yan, Yong Feng, L. Mei, 2019, Neural plasticity.

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yong Feng, Shu-shan Sang, Zhijie Niu, 2018, Journal of Human Genetics.

Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

X. Liu, D. Yan, Yong Feng, 2019, Human molecular genetics.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.